rs80356610
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in clinvar |
| Make rs80356610(C;C) |
| Make rs80356610(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 11 |
| Position | 17387968 |
| Gene | KCNJ11 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs80356610 |
| dbSNP (classic) | rs80356610 |
| ClinGen | rs80356610 |
| ebi | rs80356610 |
| HLI | rs80356610 |
| Exac | rs80356610 |
| Gnomad | rs80356610 |
| Varsome | rs80356610 |
| LitVar | rs80356610 |
| Map | rs80356610 |
| PheGenI | rs80356610 |
| Biobank | rs80356610 |
| 1000 genomes | rs80356610 |
| hgdp | rs80356610 |
| ensembl | rs80356610 |
| geneview | rs80356610 |
| scholar | rs80356610 |
| rs80356610 | |
| pharmgkb | rs80356610 |
| gwascentral | rs80356610 |
| openSNP | rs80356610 |
| 23andMe | rs80356610 |
| SNPshot | rs80356610 |
| SNPdbe | rs80356610 |
| MSV3d | rs80356610 |
| GWAS Ctlg | rs80356610 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs80356610(C;C) |
| Alt | rs80356610(C;C) |
| Reference | Rs80356610(T;T) |
| Significance | Pathogenic |
| Disease | Transient neonatal diabetes mellitus 3 Permanent neonatal diabetes mellitus Maturity-onset diabetes of the young |
| Variation | info |
| Gene | KCNJ11 |
| CLNDBN | Transient neonatal diabetes mellitus 3 Permanent neonatal diabetes mellitus Maturity-onset diabetes of the young, type 13 |
| Reversed | 1 |
| HGVS | NC_000011.9:g.17409515A>G |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000009211.4, RCV000020347.1, RCV000170298.4, |
[PMID 15784703] The C42R mutation in the Kir6.2 (KCNJ11) gene as a cause of transient neonatal diabetes, childhood diabetes, or later-onset, apparently type 2 diabetes mellitus.
